---
OA_type: closed access
_id: '21762'
abstract:
- lang: eng
  text: Bacteria, like eukaryotes, use conserved cytoskeletal systems for intracellular
    organization. The plasmid-encoded ParMRC system forms actin-like filaments that
    segregate low–copy number plasmids. In multicellular cyanobacteria such as Anabaena
    sp., we found that a chromosomally encoded ParMR system has evolved into a cytoskeletal
    system named CorMR with a function in cell shape control rather than DNA segregation.
    Live-cell imaging, in vitro reconstitution, and cryo–electron microscopy revealed
    that CorM formed dynamically unstable, antiparallel double-stranded filaments
    that were recruited to the membrane by CorR through an amphipathic helix conserved
    in multicellular cyanobacteria. CorMR filaments were regulated by MinC, which
    excluded them from the poles and division plane. Comparative genomics indicated
    that the repurposing of ParMR and Min systems coevolved with cyanobacterial multicellularity,
    highlighting the evolutionary plasticity of cytoskeletal systems in bacteria.
acknowledged_ssus:
- _id: Bio
- _id: ScienComp
- _id: EM-Fac
- _id: LifeSc
acknowledgement: "We thank all members of the Loose lab at ISTA for helpful discussions;
  M. Kojic for critical reading of the manuscript; A. Herrero (Sevilla University)
  for sharing her extensive BACTH plasmid library and other plasmids, as well as cyanobacterial
  strains; T. Dagan and F. Nies (both Kiel University) for sharing cyanobacterial
  strains and plasmids and for valuable discussions; N. Sapay and A. Michon for providing
  the Amphipaseek code, which enabled us to perform our large-scale amphipathic helix
  screen of cyanobacterial CorR proteins; V.-V. Hodirnau for support in cryo-ET data
  collection; and J. Hansen for advice about cryo-EM data processing.\r\nThis work
  was supported by the Scientific Service Units (SSU) of ISTA through resources provided
  by the Imaging & Optics Facility (IOF), the Scientific Computing (SciComp), the
  Electron Microscopy Facility (EMF), and the Lab Support Facility (LSF). This work
  was funded by the European Union’s Horizon 2020 research and innovation program
  (Marie Skłodowska-Curie grant 101034413 to B.L.S.); the European Research Council
  (ERC) of the European Union (grant ActinID 101076260 to F.K.M.S.); the Swiss National
  Science Foundation (starting grant TMSGI3_226208 to G.L.W.); and the Jean-Jacques
  et Letitia Lopez-Loreta Foundation (G.L.W.)."
article_number: eaea6343
article_processing_charge: No
article_type: original
author:
- first_name: Benjamin L
  full_name: Springstein, Benjamin L
  id: b4eb62ef-ac72-11ed-9503-ed3b4d66c083
  last_name: Springstein
  orcid: 0000-0002-3461-5391
- first_name: Manjunath
  full_name: Javoor, Manjunath
  id: 305ab18b-dc7d-11ea-9b2f-b58195228ea2
  last_name: Javoor
  orcid: 0000-0003-2311-2112
- first_name: Daniela
  full_name: Megrian, Daniela
  last_name: Megrian
- first_name: Roman
  full_name: Hajdu, Roman
  id: ffab949d-133f-11ed-8f02-94de21ace503
  last_name: Hajdu
- first_name: Dustin M.
  full_name: Hanke, Dustin M.
  last_name: Hanke
- first_name: Bettina
  full_name: Zens, Bettina
  id: 45FD126C-F248-11E8-B48F-1D18A9856A87
  last_name: Zens
  orcid: 0000-0002-9561-1239
- first_name: Gregor L.
  full_name: Weiss, Gregor L.
  last_name: Weiss
- first_name: Florian Km
  full_name: Schur, Florian Km
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
- first_name: Martin
  full_name: Loose, Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
citation:
  ama: Springstein BL, Javoor M, Megrian D, et al. Repurposing of a DNA segregation
    machinery into a cytoskeletal system controlling cell shape. <i>Science</i>. 2026;392(6795).
    doi:<a href="https://doi.org/10.1126/science.aea6343">10.1126/science.aea6343</a>
  apa: Springstein, B. L., Javoor, M., Megrian, D., Hajdu, R., Hanke, D. M., Zens,
    B., … Loose, M. (2026). Repurposing of a DNA segregation machinery into a cytoskeletal
    system controlling cell shape. <i>Science</i>. AAAS. <a href="https://doi.org/10.1126/science.aea6343">https://doi.org/10.1126/science.aea6343</a>
  chicago: Springstein, Benjamin L, Manjunath Javoor, Daniela Megrian, Roman Hajdu,
    Dustin M. Hanke, Bettina Zens, Gregor L. Weiss, Florian KM Schur, and Martin Loose.
    “Repurposing of a DNA Segregation Machinery into a Cytoskeletal System Controlling
    Cell Shape.” <i>Science</i>. AAAS, 2026. <a href="https://doi.org/10.1126/science.aea6343">https://doi.org/10.1126/science.aea6343</a>.
  ieee: B. L. Springstein <i>et al.</i>, “Repurposing of a DNA segregation machinery
    into a cytoskeletal system controlling cell shape,” <i>Science</i>, vol. 392,
    no. 6795. AAAS, 2026.
  ista: Springstein BL, Javoor M, Megrian D, Hajdu R, Hanke DM, Zens B, Weiss GL,
    Schur FK, Loose M. 2026. Repurposing of a DNA segregation machinery into a cytoskeletal
    system controlling cell shape. Science. 392(6795), eaea6343.
  mla: Springstein, Benjamin L., et al. “Repurposing of a DNA Segregation Machinery
    into a Cytoskeletal System Controlling Cell Shape.” <i>Science</i>, vol. 392,
    no. 6795, eaea6343, AAAS, 2026, doi:<a href="https://doi.org/10.1126/science.aea6343">10.1126/science.aea6343</a>.
  short: B.L. Springstein, M. Javoor, D. Megrian, R. Hajdu, D.M. Hanke, B. Zens, G.L.
    Weiss, F.K. Schur, M. Loose, Science 392 (2026).
corr_author: '1'
date_created: 2026-04-26T22:01:46Z
date_published: 2026-04-16T00:00:00Z
date_updated: 2026-04-28T13:29:05Z
day: '16'
department:
- _id: MaLo
- _id: FlSc
- _id: GradSch
- _id: EM-Fac
doi: 10.1126/science.aea6343
ec_funded: 1
external_id:
  pmid:
  - '41990175'
intvolume: '       392'
issue: '6795'
language:
- iso: eng
month: '04'
oa_version: None
pmid: 1
project:
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  call_identifier: H2020
  grant_number: '101034413'
  name: 'IST-BRIDGE: International postdoctoral program'
- _id: bd980d18-d553-11ed-ba76-ceaa645c97eb
  grant_number: '101076260'
  name: A molecular atlas of Actin filament IDentities in the cell motility machinery
publication: Science
publication_identifier:
  eissn:
  - 1095-9203
  issn:
  - 0036-8075
publication_status: published
publisher: AAAS
quality_controlled: '1'
scopus_import: '1'
status: public
title: Repurposing of a DNA segregation machinery into a cytoskeletal system controlling
  cell shape
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 392
year: '2026'
...
---
_id: '19915'
acknowledgement: "We thank all members of the Martin Loose lab at ISTA for helpful
  discussions and Marko Kojic for critical reading of the manuscript. This research
  was supported by the Scientific Service Units (SSU) of ISTA through resources provided
  by the Imaging & Optics Facility (IOF), the Scientific Computing (SciComp) and the
  Electron Microscopy Facility (EMF), as well as the Lab Support Facility (LSF). This
  project has received funding from the European Union’s Horizon 2020 research and
  innovation program under the Marie Skłodowska-Curie Grant Agreement No.101034413
  awarded to BLS as well as an ERC grant (ActinID, 101076260) from the European Union
  awarded to FKMS. Views and opinions expressed are however those of the author(s)
  only and do not necessarily reflect those of the European Union or the European
  Research Council. Neither the European Union nor the granting authority can be held
  responsible for them.\r\n\r\nWe are grateful for Antonia Herrero (Sevilla University)
  for sharing her extensive BACTH plasmid library and other plasmids as well as cyanobacterial
  strains. Likewise, we would like to thank Tal Dagan and Fabian Nies (both Kiel University)
  for sharing cyanobacterial strains and plasmids and for valuable discussions.\r\n\r\nWe
  would further like to express our gratitude to Nicolas Sapay and Alexis Michon for
  providing the Amphipaseek code, which enabled us to perform our large-scale amphipathic
  helix screen of cyanobacterial CorR proteins. Finally, we also want to thank Jesse
  Hansen for advice in cryo-EM data processing"
article_processing_charge: No
author:
- first_name: Benjamin L
  full_name: Springstein, Benjamin L
  id: b4eb62ef-ac72-11ed-9503-ed3b4d66c083
  last_name: Springstein
  orcid: 0000-0002-3461-5391
citation:
  ama: Springstein BL. Files for “Evolutionary repurposing of a DNA segregation machinery
    into a cytoskeletal system controlling cyanobacterial cell shape.” 2025. doi:<a
    href="https://doi.org/10.15479/AT:ISTA:19915">10.15479/AT:ISTA:19915</a>
  apa: Springstein, B. L. (2025). Files for “Evolutionary repurposing of a DNA segregation
    machinery into a cytoskeletal system controlling cyanobacterial cell shape.” Institute
    of Science and Technology Austria. <a href="https://doi.org/10.15479/AT:ISTA:19915">https://doi.org/10.15479/AT:ISTA:19915</a>
  chicago: Springstein, Benjamin L. “Files for ‘Evolutionary Repurposing of a DNA
    Segregation Machinery into a Cytoskeletal System Controlling Cyanobacterial Cell
    Shape.’” Institute of Science and Technology Austria, 2025. <a href="https://doi.org/10.15479/AT:ISTA:19915">https://doi.org/10.15479/AT:ISTA:19915</a>.
  ieee: B. L. Springstein, “Files for ‘Evolutionary repurposing of a DNA segregation
    machinery into a cytoskeletal system controlling cyanobacterial cell shape.’”
    Institute of Science and Technology Austria, 2025.
  ista: Springstein BL. 2025. Files for ‘Evolutionary repurposing of a DNA segregation
    machinery into a cytoskeletal system controlling cyanobacterial cell shape’, Institute
    of Science and Technology Austria, <a href="https://doi.org/10.15479/AT:ISTA:19915">10.15479/AT:ISTA:19915</a>.
  mla: Springstein, Benjamin L. <i>Files for “Evolutionary Repurposing of a DNA Segregation
    Machinery into a Cytoskeletal System Controlling Cyanobacterial Cell Shape.”</i>
    Institute of Science and Technology Austria, 2025, doi:<a href="https://doi.org/10.15479/AT:ISTA:19915">10.15479/AT:ISTA:19915</a>.
  short: B.L. Springstein, (2025).
contributor:
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  first_name: Florian KM
  id: 48AD8942-F248-11E8-B48F-1D18A9856A87
  last_name: Schur
  orcid: 0000-0003-4790-8078
- contributor_type: supervisor
  first_name: Martin
  id: 462D4284-F248-11E8-B48F-1D18A9856A87
  last_name: Loose
  orcid: 0000-0001-7309-9724
corr_author: '1'
date_created: 2025-06-27T07:34:52Z
date_published: 2025-06-27T00:00:00Z
date_updated: 2026-06-10T08:05:45Z
day: '27'
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doi: 10.15479/AT:ISTA:19915
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title: Files for "Evolutionary repurposing of a DNA segregation machinery into a cytoskeletal
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...
---
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abstract:
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  text: The synthesis of proteins as encoded in the genome depends critically on translational
    fidelity. Nevertheless, errors inevitably occur, and those that result in reading
    frame shifts are particularly consequential because the resulting polypeptides
    are typically nonfunctional. Despite the generally maladaptive impact of such
    errors, the proper decoding of certain mRNAs, including many viral mRNAs, depends
    on a process known as programmed ribosomal frameshifting. The fact that these
    programmed events, commonly involving a shift to the –1 frame, occur at specific
    evolutionarily optimized “slippery” sites has facilitated mechanistic investigation.
    By contrast, less is known about the scope and nature of error (i.e., nonprogrammed)
    frameshifting. Here, we examine error frameshifting by monitoring spontaneous
    frameshift events that suppress the effects of single base pair deletions affecting
    two unrelated test proteins. To map the precise sites of frameshifting, we developed
    a targeted mass spectrometry–based method called “translational tiling proteomics”
    for interrogating the full set of possible –1 slippage events that could produce
    the observed frameshift suppression. Surprisingly, such events occur at many sites
    along the transcripts, involving up to one half of the available codons. Only
    a subset of these resembled canonical “slippery” sites, implicating alternative
    mechanisms potentially involving noncognate mispairing events. Additionally, the
    aggregate frequency of these events (ranging from 1 to 10% in our test cases)
    was higher than we might have anticipated. Our findings point to an unexpected
    degree of mechanistic diversity among ribosomal frameshifting events and suggest
    that frameshifted products may contribute more significantly to the proteome than
    generally assumed.
acknowledgement: We thank S. L. Dove for valuable discussion and comments on the manuscript
  and R. Hellmiss for artwork. This work was supported by NIH grants GM136247 to A.H.,
  AG011085 to J.W.H., and GM132129 to J.A.P.
article_number: e2317453121
article_processing_charge: No
article_type: original
author:
- first_name: Benjamin L
  full_name: Springstein, Benjamin L
  id: b4eb62ef-ac72-11ed-9503-ed3b4d66c083
  last_name: Springstein
  orcid: 0000-0002-3461-5391
- first_name: Joao A.
  full_name: Paulo, Joao A.
  last_name: Paulo
- first_name: Hankum
  full_name: Park, Hankum
  last_name: Park
- first_name: Kemardo
  full_name: Henry, Kemardo
  last_name: Henry
- first_name: Eleanor
  full_name: Fleming, Eleanor
  last_name: Fleming
- first_name: Zoë
  full_name: Feder, Zoë
  last_name: Feder
- first_name: J. Wade
  full_name: Harper, J. Wade
  last_name: Harper
- first_name: Ann
  full_name: Hochschild, Ann
  last_name: Hochschild
citation:
  ama: Springstein BL, Paulo JA, Park H, et al. Systematic analysis of nonprogrammed
    frameshift suppression in E.coli via translational tiling proteomics. <i>Proceedings
    of the National Academy of Sciences of the United States of America</i>. 2024;121(6).
    doi:<a href="https://doi.org/10.1073/pnas.2317453121">10.1073/pnas.2317453121</a>
  apa: Springstein, B. L., Paulo, J. A., Park, H., Henry, K., Fleming, E., Feder,
    Z., … Hochschild, A. (2024). Systematic analysis of nonprogrammed frameshift suppression
    in E.coli via translational tiling proteomics. <i>Proceedings of the National
    Academy of Sciences of the United States of America</i>. National Academy of Sciences.
    <a href="https://doi.org/10.1073/pnas.2317453121">https://doi.org/10.1073/pnas.2317453121</a>
  chicago: Springstein, Benjamin L, Joao A. Paulo, Hankum Park, Kemardo Henry, Eleanor
    Fleming, Zoë Feder, J. Wade Harper, and Ann Hochschild. “Systematic Analysis of
    Nonprogrammed Frameshift Suppression in E.Coli via Translational Tiling Proteomics.”
    <i>Proceedings of the National Academy of Sciences of the United States of America</i>.
    National Academy of Sciences, 2024. <a href="https://doi.org/10.1073/pnas.2317453121">https://doi.org/10.1073/pnas.2317453121</a>.
  ieee: B. L. Springstein <i>et al.</i>, “Systematic analysis of nonprogrammed frameshift
    suppression in E.coli via translational tiling proteomics,” <i>Proceedings of
    the National Academy of Sciences of the United States of America</i>, vol. 121,
    no. 6. National Academy of Sciences, 2024.
  ista: Springstein BL, Paulo JA, Park H, Henry K, Fleming E, Feder Z, Harper JW,
    Hochschild A. 2024. Systematic analysis of nonprogrammed frameshift suppression
    in E.coli via translational tiling proteomics. Proceedings of the National Academy
    of Sciences of the United States of America. 121(6), e2317453121.
  mla: Springstein, Benjamin L., et al. “Systematic Analysis of Nonprogrammed Frameshift
    Suppression in E.Coli via Translational Tiling Proteomics.” <i>Proceedings of
    the National Academy of Sciences of the United States of America</i>, vol. 121,
    no. 6, e2317453121, National Academy of Sciences, 2024, doi:<a href="https://doi.org/10.1073/pnas.2317453121">10.1073/pnas.2317453121</a>.
  short: B.L. Springstein, J.A. Paulo, H. Park, K. Henry, E. Fleming, Z. Feder, J.W.
    Harper, A. Hochschild, Proceedings of the National Academy of Sciences of the
    United States of America 121 (2024).
date_created: 2025-01-29T08:39:27Z
date_published: 2024-02-06T00:00:00Z
date_updated: 2025-05-14T11:02:52Z
day: '06'
ddc:
- '570'
department:
- _id: MaLo
doi: 10.1073/pnas.2317453121
external_id:
  pmid:
  - '38289956'
file:
- access_level: open_access
  checksum: 5bd62c7cb4287e3706a1d45d6ef61fd1
  content_type: application/pdf
  creator: dernst
  date_created: 2025-01-29T08:43:16Z
  date_updated: 2025-01-29T08:43:16Z
  file_id: '18939'
  file_name: 2024_PNAS_Springstein.pdf
  file_size: 720902
  relation: main_file
  success: 1
file_date_updated: 2025-01-29T08:43:16Z
has_accepted_license: '1'
intvolume: '       121'
issue: '6'
language:
- iso: eng
month: '02'
oa: 1
oa_version: Published Version
pmid: 1
publication: Proceedings of the National Academy of Sciences of the United States
  of America
publication_identifier:
  eissn:
  - 1091-6490
  issn:
  - 0027-8424
publication_status: published
publisher: National Academy of Sciences
quality_controlled: '1'
scopus_import: '1'
status: public
title: Systematic analysis of nonprogrammed frameshift suppression in E.coli via translational
  tiling proteomics
tmp:
  image: /images/cc_by_nc_nd.png
  legal_code_url: https://creativecommons.org/licenses/by-nc-nd/4.0/legalcode
  name: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
    (CC BY-NC-ND 4.0)
  short: CC BY-NC-ND (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 121
year: '2024'
...
---
_id: '14785'
abstract:
- lang: eng
  text: Small cryptic plasmids have no clear effect on the host fitness and their
    functional repertoire remains obscure. The naturally competent cyanobacterium
    Synechocystis sp. PCC 6803 harbours several small cryptic plasmids; whether their
    evolution with this species is supported by horizontal transfer remains understudied.
    Here, we show that the small cryptic plasmid DNA is transferred in the population
    exclusively by natural transformation, where the transfer frequency of plasmid‐encoded
    genes is similar to that of chromosome‐encoded genes. Establishing a system to
    follow gene transfer, we compared the transfer frequency of genes encoded in cryptic
    plasmids pCA2.4 (2378 bp) and pCB2.4 (2345 bp) within and between populations
    of two <jats:italic>Synechocystis</jats:italic> sp. PCC 6803 labtypes (termed
    Kiel and Sevilla). Our results reveal that plasmid gene transfer frequency depends
    on the recipient labtype. Furthermore, gene transfer via whole plasmid uptake
    in the Sevilla labtype ranged among the lowest detected transfer rates in our
    experiments. Our study indicates that horizontal DNA transfer via natural transformation
    is frequent in the evolution of small cryptic plasmids that reside in naturally
    competent organisms. Furthermore, we suggest that the contribution of natural
    transformation to cryptic plasmid persistence in Synechocystis is limited.
acknowledgement: "We thank the lab of Francisco Javier Florencio Bel-lido, Sevilla,
  Spain for supplying theSynechocystislabtype Sevilla used in this work and the lab
  of MartinHagemann, Rostock, Germany for supplying the pIGAplasmidusedinthiswork.WethankNilsHülterforfruitful
  discussions. We thank Fenna Stücker forgraphical illustrations and Katrin Schumann,
  FennaStücker,  and  Lidusha  Manivannan  for  technicalsupport.\r\nChilean National
  Agency for Research andDevelopment (ANID), Grant/Award Number:21191763; DeutscheForschungsgemeinschaft,
  Grant/AwardNumbers: 456882089, RTG2501; EuropeanResearch Council (ERC), Grant/AwardNumber:
  101043835"
article_processing_charge: Yes (in subscription journal)
article_type: original
author:
- first_name: Fabian
  full_name: Nies, Fabian
  last_name: Nies
- first_name: Tanita
  full_name: Wein, Tanita
  last_name: Wein
- first_name: Dustin M.
  full_name: Hanke, Dustin M.
  last_name: Hanke
- first_name: Benjamin L
  full_name: Springstein, Benjamin L
  id: b4eb62ef-ac72-11ed-9503-ed3b4d66c083
  last_name: Springstein
  orcid: 0000-0002-3461-5391
- first_name: Jaime
  full_name: Alcorta, Jaime
  last_name: Alcorta
- first_name: Claudia
  full_name: Taubenheim, Claudia
  last_name: Taubenheim
- first_name: Tal
  full_name: Dagan, Tal
  last_name: Dagan
citation:
  ama: Nies F, Wein T, Hanke DM, et al. Role of natural transformation in the evolution
    of small cryptic plasmids in Synechocystis sp. PCC 6803. <i>Environmental Microbiology
    Reports</i>. 2023;15(6):656-668. doi:<a href="https://doi.org/10.1111/1758-2229.13203">10.1111/1758-2229.13203</a>
  apa: Nies, F., Wein, T., Hanke, D. M., Springstein, B. L., Alcorta, J., Taubenheim,
    C., &#38; Dagan, T. (2023). Role of natural transformation in the evolution of
    small cryptic plasmids in Synechocystis sp. PCC 6803. <i>Environmental Microbiology
    Reports</i>. Wiley. <a href="https://doi.org/10.1111/1758-2229.13203">https://doi.org/10.1111/1758-2229.13203</a>
  chicago: Nies, Fabian, Tanita Wein, Dustin M. Hanke, Benjamin L Springstein, Jaime
    Alcorta, Claudia Taubenheim, and Tal Dagan. “Role of Natural Transformation in
    the Evolution of Small Cryptic Plasmids in Synechocystis Sp. PCC 6803.” <i>Environmental
    Microbiology Reports</i>. Wiley, 2023. <a href="https://doi.org/10.1111/1758-2229.13203">https://doi.org/10.1111/1758-2229.13203</a>.
  ieee: F. Nies <i>et al.</i>, “Role of natural transformation in the evolution of
    small cryptic plasmids in Synechocystis sp. PCC 6803,” <i>Environmental Microbiology
    Reports</i>, vol. 15, no. 6. Wiley, pp. 656–668, 2023.
  ista: Nies F, Wein T, Hanke DM, Springstein BL, Alcorta J, Taubenheim C, Dagan T.
    2023. Role of natural transformation in the evolution of small cryptic plasmids
    in Synechocystis sp. PCC 6803. Environmental Microbiology Reports. 15(6), 656–668.
  mla: Nies, Fabian, et al. “Role of Natural Transformation in the Evolution of Small
    Cryptic Plasmids in Synechocystis Sp. PCC 6803.” <i>Environmental Microbiology
    Reports</i>, vol. 15, no. 6, Wiley, 2023, pp. 656–68, doi:<a href="https://doi.org/10.1111/1758-2229.13203">10.1111/1758-2229.13203</a>.
  short: F. Nies, T. Wein, D.M. Hanke, B.L. Springstein, J. Alcorta, C. Taubenheim,
    T. Dagan, Environmental Microbiology Reports 15 (2023) 656–668.
date_created: 2024-01-10T10:41:07Z
date_published: 2023-12-01T00:00:00Z
date_updated: 2024-01-16T09:46:12Z
day: '01'
ddc:
- '570'
department:
- _id: MaLo
doi: 10.1111/1758-2229.13203
external_id:
  isi:
  - '001080203100001'
  pmid:
  - '37794696'
file:
- access_level: open_access
  checksum: d09ebb68fee61f4e2e09ec286c9cf1d3
  content_type: application/pdf
  creator: dernst
  date_created: 2024-01-16T09:42:10Z
  date_updated: 2024-01-16T09:42:10Z
  file_id: '14810'
  file_name: 2023_EnvirMicroBiolReports_Nies.pdf
  file_size: 1518350
  relation: main_file
  success: 1
file_date_updated: 2024-01-16T09:42:10Z
has_accepted_license: '1'
intvolume: '        15'
isi: 1
issue: '6'
keyword:
- Agricultural and Biological Sciences (miscellaneous)
- Ecology
- Evolution
- Behavior and Systematics
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '12'
oa: 1
oa_version: Published Version
page: 656-668
pmid: 1
publication: Environmental Microbiology Reports
publication_identifier:
  eissn:
  - 1758-2229
publication_status: published
publisher: Wiley
quality_controlled: '1'
status: public
title: Role of natural transformation in the evolution of small cryptic plasmids in
  Synechocystis sp. PCC 6803
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2023'
...
